EP0323138A1 - Procédé pour la préparation d'éthers - Google Patents

Procédé pour la préparation d'éthers Download PDF

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Publication number
EP0323138A1
EP0323138A1 EP88312181A EP88312181A EP0323138A1 EP 0323138 A1 EP0323138 A1 EP 0323138A1 EP 88312181 A EP88312181 A EP 88312181A EP 88312181 A EP88312181 A EP 88312181A EP 0323138 A1 EP0323138 A1 EP 0323138A1
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EP
European Patent Office
Prior art keywords
alcohol
olefin
ether
water
fraction
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP88312181A
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German (de)
English (en)
Inventor
Tracy Jau-Hua Huang
Charles Mitchell Sorenson, Jr.
Philip Varghese
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ExxonMobil Oil Corp
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Mobil Oil Corp
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Filing date
Publication date
Application filed by Mobil Oil Corp filed Critical Mobil Oil Corp
Publication of EP0323138A1 publication Critical patent/EP0323138A1/fr
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C41/00—Preparation of ethers; Preparation of compounds having groups, groups or groups
    • C07C41/01—Preparation of ethers
    • C07C41/05—Preparation of ethers by addition of compounds to unsaturated compounds
    • C07C41/06—Preparation of ethers by addition of compounds to unsaturated compounds by addition of organic compounds only
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C41/00—Preparation of ethers; Preparation of compounds having groups, groups or groups
    • C07C41/01—Preparation of ethers
    • C07C41/09—Preparation of ethers by dehydration of compounds containing hydroxy groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C41/00—Preparation of ethers; Preparation of compounds having groups, groups or groups
    • C07C41/01—Preparation of ethers
    • C07C41/34—Separation; Purification; Stabilisation; Use of additives
    • C07C41/40—Separation; Purification; Stabilisation; Use of additives by change of physical state, e.g. by crystallisation
    • C07C41/42—Separation; Purification; Stabilisation; Use of additives by change of physical state, e.g. by crystallisation by distillation

Definitions

  • This invention relates to a process for the production of ether(s). More particularly, the invention relates to a process for the conversion of a light olefin such as ethylene, propylene, butenes, pentenes, hexenes, heptenes, etc., and their mixtures, in a conversion unit employing an acidic zeolite as olefin conversion catalyst to produce a mixture of alcohol(s) and ether(s) and thereafter recovering the ether(s) containing at most only small amounts of co-produced alcohol(s) and water.
  • a light olefin such as ethylene, propylene, butenes, pentenes, hexenes, heptenes, etc.
  • Olefin hydration employing zeolite catalysts is also known.
  • lower olefins, in particular,propylene can be catalytically hydrated over a crystalline aluminosilicate zeolite catalyst having a silica to alumina ratio of at least 12 and a Constraint Index of 1 to 12, e.g., HZSM-5, to provide the corresponding alcohol, essentially free of ether and hydrocarbon by-product.
  • an olefin is hydrated to the corresponding alcohol in the presence of hydrogen-type mordenite or hydrogen-type zeolite Y, each having a silica-alumina molar ratio of 20 to 500.
  • the use of such a catalyst is said to result in higher yields of alcohol than olefin hydration processes which employ conventional solid acid catalysts.
  • Use of the zeolite catalyst is also said to offer the advantage over ion-exchange type olefin hydration catalysts of not being restricted by the hydration temperature.
  • Reaction conditions employed in the process include a temperature of from 50-300°C, preferably 100-250°C, a pressure of 5 to 200 kg/cm2 to maintain liquid phase or gas-liquid multi-phase conditions and a mole ratio of water to olefin of from 1 to 20.
  • the reaction time can be 20 minutes to 20 hours when operating batchwise and the liquid hourly space velocity (LHSV) is usually 0.1 to 10 in the case of continuous operation.
  • LHSV liquid hourly space velocity
  • DIPE is prepared from isopropyl alcohol (IPA) employing montmorillonite clay catalysts, optionally in the presence of added propylene.
  • IPA isopropyl alcohol
  • U.S. Patent No. 4,175,210 discloses the use of silicatungstic acid as catalyst for the reaction of olefin(s) with alcohol to provide ether(s).
  • DIPE is produced from IPA and propylene in a series of operations employing a strongly acidic cation exchange resin as catalyst. In the process for producing a gasoline blending stock described in U.S. Patent No.
  • 4,418,219 describes the preparation of methyl tertiary-butyl ether (MTBE), a high octane blending agent for motor fuels, by reacting isobutylene and methanol in the presence of, as catalyst, boron phosphate, blue tungsten oxide or a crystalline aluminosilicate zeolite having a silica to alumina mole ratio of at least 12:1 and a Constraint Index of 1 to 12 as catalyst.
  • MTBE methyl tertiary-butyl ether
  • 4,605,787 discloses the preparation of alkyl tert-alkyl ethers such as MTBE and methyl tert-amyl ether (MTAE) by the reaction of a primary alcohol with an olefin having a double bond on a tertiary carbon atom employing as catalyst an acidic zeolite having a Constraint Index of 1 to 12, e.g., zeolite ZSM-5, 11, 12 and 23, dealuminized zeolite Y and rare earth-­exchanged zeolite Y.
  • 55,045 describes a process for reacting an olefin and an alcohol to provide an ether, e.g., isobutene and methanol to provide MTBE, in the presence of an acidic zeolite catalyst such as zeolite Beta and zeolites ZSM-5, 8, 11, 12, 23, 35, 43 and 48.
  • an acidic zeolite catalyst such as zeolite Beta and zeolites ZSM-5, 8, 11, 12, 23, 35, 43 and 48.
  • the invention resides in a process for producing an ether comprising:
  • the accompanying drawing is a schematic representation of a process according to one embodiment of the invention as applied to the production of DIPE.
  • the present invention is applicable to the conversion of individual light olefins and mixtures of olefins of various structure, preferably within the C2 ⁇ 7 range, to ethers. Accordingly, the invention is applicable to the conversion of ethylene, propylene, butenes, pentenes, hexenes and heptenes, mixtures of these and other olefins such as gas plant off-gas containing ethylene and propylene, naphtha cracker off-gas containing light olefins, fluidized catalytic cracked (FCC) light gasoline containing pentenes, hexenes and heptenes, refinery FCC propane/propylene streams.
  • FCC fluidized catalytic cracked
  • a typical FCC light olefin stream possesses the following composition: Typical Refinery FCC Light Olefin Composition Wt.% Mole% Ethane 3.3 5.1 Ethylene 0.7 1.2 Propane 14.5 15.3 Propylene 42.5 46.8 Isobutane 12.9 10.3 n-Butane 3.3 2.6 Butenes 22.1 18.3 Pentanes 0.7 0.4
  • the process of the invention is especially applicable to the conversion of propylene and propylene-containing streams to DIPE containing at most a minor amount of IPA.
  • the conversion of the light olefin takes place in an olefin conversion unit 11 wherein several reactions occur simultaneously to provide a mixture of alcohol and ether.
  • olefin will react with water fed to the unit 11 to produce alcohol, alcohol will react with olefin to produce ether and/or alcohol will undergo dehydration to produce ether.
  • the foregoing olefin conversion reactions can be carried out under liquid phase, vapor phase or mixed vapor-liquid phase conditions in batch or in a continuous manner under stirred tank reactor or fixed bed flow reactor conditions, e.g., trickle-bed, liquid-up-flow, liquid-down-flow, counter- current flow and co-current flow.
  • the useful olefin conversion catalysts embrace two categories of zeolite, namely, the intermediate pore size variety as represented, for example, by ZSM-5, which possess a Constraint Index (see U.S. Patent No. 4016218) of greater than about 2 and the large pore variety as represented, for example, by zeolites Y and Beta, which possess a Constraint Index no greater than about 2.
  • Both varieties of zeolites will possess a framework silica-to- alumina ratio of greater than 7, usually greater than 20.
  • the zeolite will be in the acid form and as such, will possess an alpha value of at least 1, preferably at least 10 and more preferably at least 100. It will often be advantageous to provide the zeolite as a composite bound with a catalytically active or inactive material such as alumina or silica which is stable under the olefin conversion conditions employed.
  • zeolite Beta zeolite Beta
  • X L
  • Y USY
  • REY Deal Y
  • ZSM-3 ZSM-4
  • ZSM-l2 ZSM-20
  • ZSM-50 ZSM-50
  • the olefin hydration step can be effected under essentially any practical set of hydration conditions which provides alcohol(s) and ether(s) in appreciable amounts.
  • good results can generally be obtained employing a temperature ranging from ambient (20°C) up to 300°C, preferably from 50 to 220°C and more preferably from 90 to 200°C, a total system pressure of at least about 500 kPa (5 atm), preferably at least 2000 kPa (20 atm) and more preferably at least 4000 kPa (40 atm), a water to total olefin mole ratio of 0.1 to 30, preferably 0.2 to 15 and most preferably 0.3 to 5, and an LHSV of 0.1 to 10.
  • low water:olefin mole ratios namely 0.1 - 1 and preferably 0.2 - 0.8
  • employing zeolite Beta as the catalyst shifts olefin hydration products towards ether(s) and away from alcohol(s).
  • aqueous mixture of alcohol and ether produced in the olefin conversion unit 11, together with unconverted olefin, any inert gaseous material such as saturated hydrocarbon which may have been part of the olefin feed stream and the small quantities of oligomer which are typically present in the reaction effluent are then passed to a high pressure separator unit 12 which is operated below the temperature of the olefin conversion unit 11.
  • Two liquid phases form in the high pressure separator unit 12, an aqueous phase which is recycled to the olefin conversion unit 11 and a hydrocarbon-rich phase which is flashed at lower pressure to effect separation of unconverted olefin together with any other gaseous material from the aqueous mixture of alcohol, ether and oligomer.
  • the gaseous material is recycled to the olefin conversion unit 11 with part of it being vented off if necessary to avoid build-up of inert gaseous components in the system.
  • the aqueous mixture of alcohol, ether and oligomer is then introduced into a distillation tower 13 which is preferably operated at or below atmospheric pressure to provide an azeotropic overheads fraction containing ether and minor amounts of alcohol, water and oligomer and a bottoms fraction containing water and a major part of the alcohol.
  • Part or all of the bottoms fraction is recycled to the olefin conversion unit 11 and the azeotropic overheads fraction, following condensation, is introduced into an alcohol separation unit 14 which is operated under conditions effective to provide an ether-rich fraction containing oligomer, generally in an amount of less than about 10 weight percent, and little if any alcohol and water, e.g., less than about 3 weight percent, and preferably less than 2 weight percent, of these materials individually or in combination.
  • the alcohol separation unit 14 is provided as an extraction column with process feed water serving as the extraction medium. Due to the extraction of alcohol from the ether-rich phase, the solubility of water in said phase is reduced thus leading to further loss of water from the ether product. Following extraction of the condensed azeotropic overheads from the distillation tower, the aqueous alcohol-containing extractant is introduced into the olefin conversion unit.
  • the alcohol separation unit is provided as a decanter with the condensed azeotropic overheads from the distillation tower 13 separating into an ether-rich upper phase as previously described and an aqueous alcohol phase which is recycled to the olefin conversion unit 11.
  • the zeolite olefin conversion catalyst employed in these examples is zeolite Beta (82.5 wt.%) extrudate bound with colloidal silica (17.5 wt.%).
  • the extrudate was prepared by thoroughly mixing the zeolite and colloidal silica together with a sufficient amount of water to provide an extrudable mass in the absence of any added alkali metal base and/or basic salt. Extrusion of the mass into 1/16 ⁇ (1.6mm) average diameter extrudate was followed by drying, calcining, ammonium-exchange and calcining in the conventional manner to provide an activated catalyst.
  • silica-bound zeolite Beta catalyst was employed in the conversion of propylene to a mixture of IPA and DIPE under the following fixed conditions: 166°C (330°F), 7000 kPa (1000 psig) total system pressure and 0.5 weight hourly velocity (WHSV) based on propylene.
  • the amount of IPA recycle was varied from 0.0 to 0.8, the effect of recycle on DIPE production being shown in Table 1 below as follows: Table 1 Effect of IPA Recycle on DIPE Production Example IPA WHSV Propylene Conversion, % DIPE Wt% Yield 1 0.0 44 26 2 0.04 35 21 3 0.3 28 38 4 0.8 23 36

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Catalysts (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
EP88312181A 1987-12-30 1988-12-22 Procédé pour la préparation d'éthers Withdrawn EP0323138A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US139566 1980-04-11
US07/139,566 US4906787A (en) 1987-12-30 1987-12-30 Process for the production of ethers

Publications (1)

Publication Number Publication Date
EP0323138A1 true EP0323138A1 (fr) 1989-07-05

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Application Number Title Priority Date Filing Date
EP88312181A Withdrawn EP0323138A1 (fr) 1987-12-30 1988-12-22 Procédé pour la préparation d'éthers

Country Status (6)

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US (1) US4906787A (fr)
EP (1) EP0323138A1 (fr)
JP (1) JPH01213248A (fr)
CN (1) CN1018178B (fr)
AU (1) AU612751B2 (fr)
ZA (1) ZA889604B (fr)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0424154A1 (fr) * 1989-10-20 1991-04-24 Mobil Oil Corporation Procédé intégré pour la production de l'éther di-isopropylique et de l'essence
EP0448998A1 (fr) * 1990-03-28 1991-10-02 Mobil Oil Corporation Préparation d'éthyl terioalkyl éthers
EP0458048A1 (fr) * 1990-05-24 1991-11-27 Mobil Oil Corporation Fabrication de l'éther diisopropylique
WO1992001660A1 (fr) * 1990-07-25 1992-02-06 Mobil Oil Corporation Hydratation catalytique amelioree d'olefines pour la production d'ether
EP0652200A1 (fr) * 1993-11-08 1995-05-10 Texaco Development Corporation Génération d'éthers à partir d'acétone
EP0665207A1 (fr) * 1994-01-28 1995-08-02 Texaco Development Corporation Production d'alcool isopropylique et d'éthers à partir d'acétone
EP0733615A1 (fr) * 1995-03-20 1996-09-25 Uop Procédé pour la production de l'éther diisopropylique
US5569789A (en) * 1994-12-01 1996-10-29 Mobil Oil Corporation Multistage indirect propylene hydration process for the production of diisopropyl ether and isopropanol

Families Citing this family (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH028873B2 (fr) * 1980-08-04 1990-02-27 Furitsutsu Aizenringu
US4935552A (en) * 1989-01-12 1990-06-19 Mobil Oil Corporation Dual stage process for the production of ethers
US5130101A (en) * 1989-04-28 1992-07-14 Mobil Oil Corporation Reactor system for conversion of alcohols to ether-rich gasoline
US5015783A (en) * 1989-12-04 1991-05-14 Uop Production of ethers by the reaction of alcohols and olefins
US5113024A (en) * 1991-06-07 1992-05-12 Mobil Oil Corporation Process for product separation in the production of di-isopropyl ether
US5208387A (en) * 1991-12-27 1993-05-04 Mobil Oil Corporation Two stage process for production of diisopropyl ether
US5288924A (en) * 1992-09-18 1994-02-22 Mobil Oil Corporation Process for starting up an olefin hydration reactor
US5313006A (en) * 1992-12-21 1994-05-17 Texaco Chemical Company Cogeneration of isobutylene plus MTBE from crude t-butanol/methanol feedstocks
US5324865A (en) * 1993-02-22 1994-06-28 Mobil Oil Corporation Di-isopropyl ether production
US5324866A (en) * 1993-03-23 1994-06-28 Uop Integrated process for producing diisopropyl ether from isopropyl alcohol
US5371301A (en) * 1993-06-21 1994-12-06 Uop Single stage diisopropyl ether process using aqueous extraction and ion exchange treating for SO3 removal
US5600023A (en) * 1993-06-21 1997-02-04 Uop Single stage diisopropyl ether process using organic solvent aqueous extraction and ion exchange treating for SO3 removal
US5986148A (en) * 1993-08-02 1999-11-16 Mobil Oil Corporation Di-isopropyl ether synthesis and dry product recovery
US5399788A (en) * 1993-12-22 1995-03-21 Uop Two-stage process for producing diisopropyl ether using hydration
US5637778A (en) * 1994-08-08 1997-06-10 Texaco Chemical Inc. Isopropyl alcohol and diispropyl ether production from crude by-product acetone in one step
US5571387A (en) * 1994-09-13 1996-11-05 Uop Continuous single vessel distillation and adsorption process
US5473105A (en) * 1994-10-04 1995-12-05 Uop Process for concurrently producing diisopropyl ether and isoproyl ethyl ether
US5565066A (en) * 1994-10-07 1996-10-15 Uop Single vessel distillation and adsorption apparatus
US5585527A (en) * 1994-10-31 1996-12-17 Uop Continuous distillation and membrane process
US5614065A (en) * 1994-10-31 1997-03-25 Uop Distillation with membrane apparatus
US5684213A (en) * 1996-03-25 1997-11-04 Chemical Research & Licensing Company Method for the preparation of dialkyl ethers
US6028183A (en) 1997-11-07 2000-02-22 Gilead Sciences, Inc. Pyrimidine derivatives and oligonucleotides containing same
US6069284A (en) * 1998-06-17 2000-05-30 Uop Llc Process for separating diisopropyl ether from isopropyl alcohol and water
WO2009137282A1 (fr) * 2008-05-09 2009-11-12 Dow Global Technologies Inc. Procédé d’éthérification des oléfines
CN101955418B (zh) * 2009-12-16 2013-10-16 华东理工大学 一种耦合分离纯化制备etbe的方法
CN114364652A (zh) * 2019-09-30 2022-04-15 陶氏环球技术有限责任公司 醚化方法
CN113717034B (zh) * 2021-10-08 2023-03-28 河北工业大学 一种固体催化剂催化精馏选择性制备二元醇单叔丁醚的方法

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3989762A (en) * 1969-04-03 1976-11-02 Veba-Chemie Ag Process for the manufacture of alcohols by the hydration of olefins
US4334890A (en) * 1981-02-03 1982-06-15 The Halcon Sd Group, Inc. Process for gasoline blending stocks
US4605787A (en) * 1984-08-16 1986-08-12 Mobil Oil Corporation Process for the preparation of alkyl tert-alkyl ethers
EP0210793A1 (fr) * 1985-07-17 1987-02-04 The British Petroleum Company p.l.c. Procédé de préparation d'un produit d'hydratation à partir d'un produit initial oléfinique
EP0213884A2 (fr) * 1985-09-03 1987-03-11 Mobil Oil Corporation Fabrication d'éthers à partir d'oléfines linéaires

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3116780A1 (de) * 1981-04-28 1982-11-04 Veba Oel AG, 4660 Gelsenkirchen-Buer Verfahren zur herstellung von sec.-butylalkohol und sec.-butyl-tert.-butylether
JPS5965025A (ja) * 1982-09-03 1984-04-13 デュオリト・アンテルナショナル・ソシエテ・アノニム スルホン化された強酸性のイオン交換樹脂触媒を用いる可逆反応
GB8606385D0 (en) * 1986-03-14 1986-04-23 Ici Plc Gasoline blending components
US4820877A (en) * 1987-12-28 1989-04-11 Mobil Oil Corporation Etherification process improvement
US4814519A (en) * 1987-12-30 1989-03-21 Mobil Oil Corporation Production of ethers from olefins
EP0323137A1 (fr) * 1987-12-30 1989-07-05 Mobil Oil Corporation Procédé pour la préparation d'éthers

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3989762A (en) * 1969-04-03 1976-11-02 Veba-Chemie Ag Process for the manufacture of alcohols by the hydration of olefins
US4334890A (en) * 1981-02-03 1982-06-15 The Halcon Sd Group, Inc. Process for gasoline blending stocks
US4605787A (en) * 1984-08-16 1986-08-12 Mobil Oil Corporation Process for the preparation of alkyl tert-alkyl ethers
EP0210793A1 (fr) * 1985-07-17 1987-02-04 The British Petroleum Company p.l.c. Procédé de préparation d'un produit d'hydratation à partir d'un produit initial oléfinique
EP0213884A2 (fr) * 1985-09-03 1987-03-11 Mobil Oil Corporation Fabrication d'éthers à partir d'oléfines linéaires

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0424154A1 (fr) * 1989-10-20 1991-04-24 Mobil Oil Corporation Procédé intégré pour la production de l'éther di-isopropylique et de l'essence
EP0448998A1 (fr) * 1990-03-28 1991-10-02 Mobil Oil Corporation Préparation d'éthyl terioalkyl éthers
EP0458048A1 (fr) * 1990-05-24 1991-11-27 Mobil Oil Corporation Fabrication de l'éther diisopropylique
US5154801A (en) * 1990-05-24 1992-10-13 Mobil Oil Corporation Advances in product separation in dipe process
AU636213B2 (en) * 1990-05-24 1993-04-22 Mobil Oil Corporation Production of diisopropyl ether
WO1992001660A1 (fr) * 1990-07-25 1992-02-06 Mobil Oil Corporation Hydratation catalytique amelioree d'olefines pour la production d'ether
US5162591A (en) * 1990-07-25 1992-11-10 Mobil Oil Corporation Catalytic olefin hydration for ether production
AU642297B2 (en) * 1990-07-25 1993-10-14 Mobil Oil Corporation Improved catalytic olefin hydration for ether production
EP0652200A1 (fr) * 1993-11-08 1995-05-10 Texaco Development Corporation Génération d'éthers à partir d'acétone
EP0665207A1 (fr) * 1994-01-28 1995-08-02 Texaco Development Corporation Production d'alcool isopropylique et d'éthers à partir d'acétone
US5569789A (en) * 1994-12-01 1996-10-29 Mobil Oil Corporation Multistage indirect propylene hydration process for the production of diisopropyl ether and isopropanol
EP0733615A1 (fr) * 1995-03-20 1996-09-25 Uop Procédé pour la production de l'éther diisopropylique

Also Published As

Publication number Publication date
US4906787A (en) 1990-03-06
AU2761388A (en) 1989-07-06
ZA889604B (en) 1990-08-29
CN1034532A (zh) 1989-08-09
AU612751B2 (en) 1991-07-18
CN1018178B (zh) 1992-09-09
JPH01213248A (ja) 1989-08-28

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